"68999-438-24" National Drug Code (NDC)

NDC Code	68999-438-24
Package Description	2 TRAY in 1 BOX (68999-438-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-438-05)
Product NDC	68999-438
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tricitrates
Non-Proprietary Name	Tricitrates
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20221208
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Chartwell Governmental & Specialty RX, LLC.
Substance Name	CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE; SODIUM CITRATE
Strength	334; 550; 500
Strength Unit	mg/5mL; mg/5mL; mg/5mL
Pharmacy Classes	Acidifying Activity [MoA], Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]